Exact Mass: 884.4686837999999
Exact Mass Matches: 884.4686837999999
Found 60 metabolites which its exact mass value is equals to given mass value 884.4686837999999,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Gracillin
Gracillin is a triterpenoid. Gracillin is a natural product found in Dracaena draco, Clintonia udensis, and other organisms with data available. Gracillin is a steroidal saponin extracted from the roots of the plant and has anti-tumor properties. Gracillin is a steroidal saponin extracted from the roots of the plant and has anti-tumor properties.
Deltonin
Deltonin is a triterpenoid. Deltonin is a natural product found in Ophiopogon planiscapus, Allium vineale, and other organisms with data available. Deltonin is found in onion-family vegetables. Deltonin is a constituent of Allium vineale (wild garlic) Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis, has antitumor activity; Deltonin inhibits ERK1/2 and AKT activation. Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis, has antitumor activity; Deltonin inhibits ERK1/2 and AKT activation. Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis, has antitumor activity; Deltonin inhibits ERK1/2 and AKT activation.
Polypodoside A
Polypodoside A is a constituent of rhizomes of the licorice fern (Polypodium glycyrrhiza). Intensely sweet substance. Constituent of rhizomes of the licorice fern (Polypodium glycyrrhiza). Intensely sweet substance.
Diosgenin 3-[glucosyl-(1->4)-rhamnosyl-(1->4)-glucoside]
Diosgenin 3-[glucosyl-(1->4)-rhamnosyl-(1->4)-glucoside] is found in onion-family vegetables. Diosgenin 3-[glucosyl-(1->4)-rhamnosyl-(1->4)-glucoside] is a constituent of Allium vineale (wild garlic).
Melongoside H
Melongoside H is found in fruits. Melongoside H is a constituent of Solanum melongena (aubergine). Constituent of Solanum melongena (aubergine). Melongoside H is found in fruits and eggplant.
Graecunin G
Isolated from the leaves of Trigonella foenum-graecum (fenugreek). Graecunin G is found in herbs and spices and fenugreek. Graecunin G is found in fenugreek. Graecunin G is isolated from the leaves of Trigonella foenum-graecum (fenugreek).
beta-Chacotriosyllilagen
beta-Chacotriosyllilagen is found in onion-family vegetables. beta-Chacotriosyllilagen is a constituent of Allium tuberosum (Chinese chives)
Gracillin
PI(16:2(9Z,12Z)/PGJ2)
C45H73O15P (884.4686837999999)
PI(16:2(9Z,12Z)/PGJ2) is an oxidized phosphatidylinositol (PI). Phosphatidylinositols are important lipids, both as a key membrane constituent and as a participant in essential metabolic processes, both directly and via a number of metabolites. Phosphatidylinositols are acidic (anionic) phospholipids that consist of a phosphatidic acid backbone, linked via the phosphate group to inositol (hexahydroxycyclohexane). Phosphatidylinositols can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. PI(16:2(9Z,12Z)/PGJ2), in particular, consists of one chain of 9Z,12Z-hexadecenoyl at the C-1 position and one chain of Prostaglandin J2 at the C-2 position. The inositol group that is part of every phosphatidylinositol lipid is covalently linked to the phosphate group that acts as a bridge to the lipid tail. In most organisms, the stereochemical form of this inositol is myo-D-inositol (with one axial hydroxyl in position 2 with the remainder equatorial), although other forms can be found in certain plant phosphatidylinositols. Phosphatidylinositol is especially abundant in brain tissue, where it can amount to 10\\% of the phospholipids, but it is present in all tissues and cell types. There is usually less of it than of phosphatidylcholine, phosphatidylethanolamine and phosphatidylserine. In animal tissues, phosphatidylinositol is the primary source of the arachidonic acid required for biosynthesis of eicosanoids, including prostaglandins, via the action of the enzyme phospholipase A2. Phosphatidylinositol can be phosphorylated by a number of different kinases that place the phosphate moiety on positions 4 and 5 of the inositol ring, although position 3 can also be phosphorylated by a specific kinase. Seven different isomers are known, but the most important in both quantitative and biological terms are phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate. Phosphatidylinositol and the phosphatidylinositol phosphates are the main source of diacylglycerols that serve as signaling molecules, via the action of phospholipase C enzymes. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PIs composed exclusively of non-phosphorylated inositol exhibit a net charge of -1 at physiological pH. Molecules with phosphorylated inositol (such as PIP, PIP2, PIP3, etc.) are termed polyphosphoinositides. The polyphosphoinositides are important intracellular transducers of signals emanating from the plasma membrane. The synthesis of PI involves CDP-activated 1,2-diacylglycerol condensation with myo-inositol.
PI(PGJ2/16:2(9Z,12Z))
C45H73O15P (884.4686837999999)
PI(PGJ2/16:2(9Z,12Z)) is an oxidized phosphatidylinositol (PI). Phosphatidylinositols are important lipids, both as a key membrane constituent and as a participant in essential metabolic processes, both directly and via a number of metabolites. Phosphatidylinositols are acidic (anionic) phospholipids that consist of a phosphatidic acid backbone, linked via the phosphate group to inositol (hexahydroxycyclohexane). Phosphatidylinositols can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. PI(PGJ2/16:2(9Z,12Z)), in particular, consists of one chain of Prostaglandin J2 at the C-1 position and one chain of 9Z,12Z-hexadecenoyl at the C-2 position. The inositol group that is part of every phosphatidylinositol lipid is covalently linked to the phosphate group that acts as a bridge to the lipid tail. In most organisms, the stereochemical form of this inositol is myo-D-inositol (with one axial hydroxyl in position 2 with the remainder equatorial), although other forms can be found in certain plant phosphatidylinositols. Phosphatidylinositol is especially abundant in brain tissue, where it can amount to 10\\% of the phospholipids, but it is present in all tissues and cell types. There is usually less of it than of phosphatidylcholine, phosphatidylethanolamine and phosphatidylserine. In animal tissues, phosphatidylinositol is the primary source of the arachidonic acid required for biosynthesis of eicosanoids, including prostaglandins, via the action of the enzyme phospholipase A2. Phosphatidylinositol can be phosphorylated by a number of different kinases that place the phosphate moiety on positions 4 and 5 of the inositol ring, although position 3 can also be phosphorylated by a specific kinase. Seven different isomers are known, but the most important in both quantitative and biological terms are phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate. Phosphatidylinositol and the phosphatidylinositol phosphates are the main source of diacylglycerols that serve as signaling molecules, via the action of phospholipase C enzymes. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PIs composed exclusively of non-phosphorylated inositol exhibit a net charge of -1 at physiological pH. Molecules with phosphorylated inositol (such as PIP, PIP2, PIP3, etc.) are termed polyphosphoinositides. The polyphosphoinositides are important intracellular transducers of signals emanating from the plasma membrane. The synthesis of PI involves CDP-activated 1,2-diacylglycerol condensation with myo-inositol.
Pennogenin triglycoside
Pennogenin 3-O-beta-chacotrioside is a natural product found in Ypsilandra thibetica, Triteleia hyacinthina, and other organisms with data available. Pennogenin 3-O-beta-chacotrioside is an active component isolated from Paris polyphylla, modulates autophagy via increasing the expressions of autophagy-related proteins LC3 and Beclin-1. Anti-colorectal cancer activity[1]. Pennogenin 3-O-beta-chacotrioside is an active component isolated from Paris polyphylla, modulates autophagy via increasing the expressions of autophagy-related proteins LC3 and Beclin-1. Anti-colorectal cancer activity[1].
Pennogenin
Pennogenin 3-O-beta-chacotrioside is a natural product found in Ypsilandra thibetica, Triteleia hyacinthina, and other organisms with data available. Pennogenin 3-O-beta-chacotrioside is an active component isolated from Paris polyphylla, modulates autophagy via increasing the expressions of autophagy-related proteins LC3 and Beclin-1. Anti-colorectal cancer activity[1]. Pennogenin 3-O-beta-chacotrioside is an active component isolated from Paris polyphylla, modulates autophagy via increasing the expressions of autophagy-related proteins LC3 and Beclin-1. Anti-colorectal cancer activity[1].
(25S)-spirostan-5-ene-3beta,21-diol-3-O-alpha-L-rhamnopyranosyl-(1,2)-[alpha-L-rhamnopyranosyl-(1,4)]-beta-D-glucopyranoside|yamogenin II
(25R)-Spirost-5-en-3beta,14alpha-diol-3-O-(2-O-alpha-L-rhamnopyranosyl)(4-O-alpha-L-rhamnopyranosyl)-beta-D-glucopyranosid|25(R)-dracaenoside G
(25R,26R)-26-Methoxyspirost-5-en-3beta-ol 3-O-alpha-L-rhamnopyranosyl-(1->2)-O-3)>-beta-D-glucopyranoside|(25R,26R)-26-Methoxyspirost-5-en-3beta-ol 3-O-alpha-L-rhamnopyranosyl-(1->2)-O-[alpha-L-arabinopyranosyl-(1->3)]-beta-D-glucopyranoside
3-O-<(beta-D-glucopyranosyl(1->3))(alpha-L-rhamnopyranosyl(1->4))beta-D-glucopyranosyl>-(25S)-spirost-5-en-3beta-ol|3-O-{[beta-D-glucopyranosyl(1->3)][alpha-L-rhamnopyranosyl(1->4)]beta-D-glucopyranosyl}-(25S)-spirost-5-en-3beta-ol
26-O-beta-D-glucopyranose-3beta,26-diol-(25R)-Delta5,20(22)-3-O-{[alpha-L-(25R)-pyranorhamnose(1-4)]-beta-D-glucopyranoside}
(25R)-17alpha-hydroxyspirost-5-en-3beta-yl alpha-L-rhamnopyranosyl-(1->4)-alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranoside|(3beta,17alpha,25R)-spirost-5-ene-3,17-diol-3-O-alpha-L-rhamnopyranosyl-(1->4)-alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranoside|pennogenin 3-O-alpha-L-rhamnopyranosyl(1?4)-alpha-L-rhamnopyranosyl(1?4)-beta-D-glucopyranoside|pennogenin 3-O-alpha-L-rhamnopyranosyl-(1->4)-alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranoside
2beta,3beta,17,23-tetrahydroxy-28-norolean-12-en-16-one-3-O-alpha-L-arabinopyranosyl(1-2)-alpha-L-arabinopyranosyl(1-6)-beta-D-glucopyranoside
nuatigenin 3-O-2)-O-4)>-beta-D-glucopyranoside>|nuatigenin 3-O-{O-alpha-L-rhamnopyranosyl-(1-->2)-O-[alpha-L-rhamnopyranosyl-(1-->4)]-beta-D-glucopyranoside}
3-O-{alpha-L-rhamnopyranoside(1?2)-O-[alpha-L-rhamnopyranoside(1?3)]-beta-D-glucopyranosyl}(1,3,22R,25S)-spirost-5-ene-1beta,3beta-diol|drangustoside A
ruscogenin-1-O-[beta-D-glucopyranosyl(1->2)]-[beta-D-xylopyranosyl(1->3)]-beta-D-fucopyranoside
(25R)-spirost-5-en-3beta-yl O-alpha-L-rhamnopyranosyl-(1->2)-O-6)>-beta-D-glucopyranoside|(25R)-spirost-5-en-3beta-yl O-beta-D-glucopyranosyl-(1->6)-[O-alpha-L-rhamnopyranosyl(1->2)]-beta-D-glucopyranoside|(3beta,25R)-spirost-5-en-3-ol 3-O-beta-D-glucopyranosyl-(1?6)-[alpha-L-rhamnopyranosyl-(1?2)]-beta-D-glucopyranoside
(25R)-1alpha-hydroxyspirost-5-en-3beta-yl O-alpha-L-rhamnopyranosyl-(1->2)-[O-alpha-L-rhamnopyranosyl(1->4)]-beta-D-glucopyranoside
(24S,25R)-24-Hydroxyspirost-5-en-3??-yl O-??-L-rhamnopyranosyl-(1鈥樏傗垎2)-O-[??-L-rhamnopyranosyl-(1鈥樏傗垎3)]-??-D-glucopyranoside
Furostan, β-D-glucopyranoside deriv
Furostan, |A-D-glucopyranoside deriv is a natural product found in Dioscorea panthaica with data available.
Polypodoside A
b-Chacotriosyllilagen
GRAECUNIN G
Melongoside H
Diosgenin 3-[glucosyl-(1->4)-rhamnosyl-(1->4)-glucoside]
3-O-(Rhaa1-2Glcb)-26-O-(Glcb)-(25R)-furosta-5,20(22)-dien-3beta,26-diol
3-O-(Rhaa1-2(Glcb1-4)Glcb)-(25R)-spirost-5en-3beta-ol
[6-[2-[(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoyl]oxy-3-[(3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoyl]oxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid
[(2S,3S,6S)-6-[2-[(5E,7E,9E,11E,13E)-hexadeca-5,7,9,11,13-pentaenoyl]oxy-3-[(6E,9E,12E,15E,18E,21E)-tetracosa-6,9,12,15,18,21-hexaenoyl]oxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid
Deltonin
Deltonin is a triterpenoid. Deltonin is a natural product found in Ophiopogon planiscapus, Allium vineale, and other organisms with data available. Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis, has antitumor activity; Deltonin inhibits ERK1/2 and AKT activation. Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis, has antitumor activity; Deltonin inhibits ERK1/2 and AKT activation. Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis, has antitumor activity; Deltonin inhibits ERK1/2 and AKT activation.